ZMP
si:dkey-183c23.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate golgi-specific brefeldin A resistance factor 1 (GBF1) [Source:Un
Human Orthologue:
GBF1
Human Description:
golgi brefeldin A resistant guanine nucleotide exchange factor 1 [Source:HGNC Symbol;Acc:4181]
Mouse Orthologue:
Gbf1
Mouse Description:
golgi-specific brefeldin A-resistance factor 1 Gene [Source:MGI Symbol;Acc:MGI:1861607]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12707 | Nonsense | Available for shipment | Available now |
sa18494 | Nonsense | Available for shipment | Available now |
sa9693 | Nonsense | Available for shipment | Available now |
sa14258 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12707
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046792 | Nonsense | 154 | 1786 | 5 | 38 |
ENSDART00000141695 | Nonsense | 206 | 601 | 8 | 15 |
ENSDART00000146592 | None | None | 1177 | None | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 6555601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7348759 |
GRCz11 | 13 | 7680961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACGTGTGTCTCTGCAGATTGCCACAGTTCAAAGAGGAGGCCAAGAGTTA[T/A]GTGGGCACTAACATGAAGAAGGTAAATATRAAATCCTTTTTGCTATCCAT
Long Flanking Sequence:
CTAGGGCAGTGGTGCTCAACCCTGTTCCTGGAGATCGACCTTCCTACAAACTTCAGCTCCAACCTTGATCAAACACACCTGAACCAATTAATTAGGACCTGAACAGCACTTGATAATTACTGGCAGGTGTGTTTGATATAAGTTGCAACTGAAATCAGCAAGAGTGTCGATTTCCAGGTACAGGGTTGTTCACGCCTGGTGTAGGGGGTCGAATCGGGATCGCAATCTTTTTTCGATTAATTGTGCAGCTCTACGTCATAGTGGTTACGTCAACGTCAAGCTGTAACATAATATATTGGTTCCATTGGTTTATTATTGTTATTCATTTGGGCGGCTTAAATGCTTTGTGGGTGAGTTATTTGTCACTATTTAAAACGGACCTGTAAAAAAATAAAAAATTAAACTTGTTGCTATAAATGCATTCAAATATCTAGCAAACTGTAACGCATGTACGTGTGTCTCTGCAGATTGCCACAGTTCAAAGAGGAGGCCAAGAGTTA[T/A]GTGGGCACTAACATGAAGAAGGTAAATATAAAATCCTTTTTGCTATCCATTCTCCCCTAGTCCCTCTACACCTGTTTCCCATCTGCCTTCTCATTTCCTTTATGAGCTTTGTTACGTAGAGGTCTTCATACCCATAAGTGAGGTCAGTTGCTGTTGCATAATTATTATACCTGTGTGTGTATGCGCGTGCGTGTCATCCATCAGGTCACAAAATAGAAAGTAGTAGTGAGAGTTAACAGTGTTTCACAGCTACTGTCGATTCTTTATTTGAAAGACTTCTGCTCCTTTTCATTGCAGTTATTCAAGGATTAGAATCTTCTTTCTTTTCATACCTGTTTGTTGTCTTTGAGTTCATCCTTTACCCGTTTGCCTGTTCCAACTCGCAGATCCCAGGCTGTATTCTGGACGCACAGGATTTTATTTATGCAGATCAGCCTAGAAACACCAATCAGACGGGCTTAGAGAGGGTATAGCACATTTCCATGCATTAAAACAGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18494
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046792 | Nonsense | 740 | 1786 | 16 | 38 |
ENSDART00000141695 | None | None | 601 | None | 15 |
ENSDART00000146592 | Nonsense | 129 | 1177 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 6533905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7370455 |
GRCz11 | 13 | 7702657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTGTATCTGGAGGCTTTCCGTCTTCCTGGCGAAGCGCCTGTCATTCAT[C/T]GACTTTTGGAAACCTTCACYGACAACTGGCATGTAAGTCAGCTGCCACAC
Long Flanking Sequence:
AAATCCTTAGCGTTAAACCCTGATATATATGATTTTCTAAAGTAGTAGTGTTTTGAAATTGATGAATGCATAATAATCATAATCAGTATAACCATAAAACCGTGAGTATTCCTTAGACTTTAATAATACAACCAAACTCTATAATCATTGCATCCCTAATCTGGCATACACCACAGCTCAGTAGAAACAAGGCATTAGATTTGCTGGGTCTGTTAACTCAGTTGAGTTGATTGTCCTTTCAACATTCACCAACACAACCCTAGTTTAACACCTGAAATGAAATACTGTCCTTAAGCTTTGGATGTTCTTCTCACTGTAAATTACTAGCAGCCTCAAAGTGACTGTCAGTTTGGAGTTTGAGATAATTATGCCTTAAGTGGTTTTAATGCCATCTCTGTCTCTTCCTCAGCACGTTCACCTTCCAGGGTCTGCGCATAGACGAGGCCCTCCGCTTGTATCTGGAGGCTTTCCGTCTTCCTGGCGAAGCGCCTGTCATTCAT[C/T]GACTTTTGGAAACCTTCACTGACAACTGGCATGTAAGTCAGCTGCCACACGCATACACAAGCATGGGCTGGCAGGGACTGAAGTGAATATATATATATATACACACTCTGGAGCGGGAACACACACATATACTCTTTAAATAGGTAGTAGGTTCGCTGCAGTCACAGACACAAGCATTCTTACAGTTCTTCCATTACCACACTCCAAGGCAATCCTGGCCACCAACTGGCCCCATCATCAGGTAATTAGGGACAGTGGAATAGCTCTTGGGATCAAGGACAGGGTCATTAGTCACGCAGGTAATCGGGGAAGAGGAAAATGTTGCACCGGGAAGTGAGACACATCCATCCGCCCCGCAGAAAGCAGCTCAGGCGATCCGAGGACATATCCAACAGGCTCACTTATGTGCTTATTAAAAGCGGTGCTCTCTGAGTGACCTGGAAAGTATTCGTAGTAATTTCTTTTCTTAGTCGCCATTCTCGATCTCTACGAATGAGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9693
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046792 | Nonsense | 768 | 1786 | 17 | 38 |
ENSDART00000141695 | None | None | 601 | None | 15 |
ENSDART00000146592 | Nonsense | 157 | 1177 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 6533107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7371253 |
GRCz11 | 13 | 7703455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAACGGTAATCCCTTCCAGACAAATGACGCTGGCTTCGCCCTGGCTTA[C/A]GCCGTGATCATGYTWAACACCGATCAGCACAACCATAACGTTCGAAAGCA
Long Flanking Sequence:
AGGTAATCGGGGAAGAGGAAAATGTTGCACCGGGAAGTGAGACACATCCATCCGCCCCGCAGAAAGCAGCTCAGGCGATCCGAGGACATATCCAACAGGCTCACTTATGTGCTTATTAAAAGCGGTGCTCTCTGAGTGACCTGGAAAGTATTCGTAGTAATTTCTTTTCTTAGTCGCCATTCTCGATCTCTACGAATGAGCTCATGTGATTATGCCACACAGACGCGCGGGTCGCGCCCTCCCCGATGGCAATGTATCGAAACTGGAAGGGATTCAGTTTCTGACATTTACACTTGCAGGAGATCCCTGAGGAATTACCGTGCCCTTTTATATTTTTCTTGTGGCGAATGATTTGAGTCTGTAAAGATAAGTGTACATATTAGGTGATTTGATCATGCTATTCTTGCACTCAGAGTCAGGTATATGGCCTTGTTCTTTTGTGTGCAGAAAGTGAACGGTAATCCCTTCCAGACAAATGACGCTGGCTTCGCCCTGGCTTA[C/A]GCCGTGATCATGTTAAACACCGATCAGCACAACCATAACGTTCGAAAGCAGAACATCCCCATGACTTTGGAGGTGAGTGACGCATGTTCCTTCTACAGATGCAGAAAAAAATCACATGTTCAGAGCTACAGACGCAATCTCTGTGTCAGATCAGTTTCAGCTATATGACTTAACAGTATAAGATAAGTGTATTACGTGTTTTTCTTGTAAGTGTGTTATGAAACTAGATTGCCTAGATTTACCACACATAAAGATTACTGTTATGTAGCCATGCCTCACTTCTATGTGCTTTAAGCAGCTGGCCTCGGTTTTATAGAGCTGTGAGCTTACAGTATATGAAAAAATCAGTCACGGCAGTCACACATAGACATTTTAATGAGTGTACATGTGTCATTTAAAGAAATACTTTATCAAGAAGAACTACAAAAACATGCTGTGAACCTCACCAAATCCAATTCATTTCACAACAATAATATAGAGAAAAGGCTTACATTTTGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14258
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046792 | Essential Splice Site | 820 | 1786 | 18 | 38 |
ENSDART00000141695 | None | None | 601 | None | 15 |
ENSDART00000146592 | Essential Splice Site | 209 | 1177 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 6528945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7375415 |
GRCz11 | 13 | 7707617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATGACTTTGATCAAGATATGCTGGAAGACATCTACAATGCCATCAAG[T/C]TAGTGCTCATTGTCTTGTTGTTCTCTTGCAGTTGTTGCTCTTTCTAATRC
Long Flanking Sequence:
TTGTGTGTGTGTGTGTGTGTGTGTGCGTTTACTCCCTCTCTCCAGCCATGGAAAATGCAGTCCTGGAAAGACCCTCTGTTTACTCCTCTGTTTATTTCTCCTTCTGTTCATCCCTCTCTCGGGGGGAGGAAGCTCAGGTTTCCCTTGCTTTACCTGCCATTAAGAAAGTATGCAGTAAAACAGTGGCCTAACGCCATCACTCAGCAGCGGACGTCTGTGTGTTTATTTGAGCTGAGCTTGGCCTTAGACCAGCCTGCTTAACACTAACACCTATTAAGTGACACCAGCAGTAATAAACCGAGACCAATTATTGGATTTGAAAGGCGATAGTTGGAGGATGTCGCCGTAATTGGATGGAATGAAGGCATTTTAATCAGTTTCCTCCTCCTGTTTGTTGTTTTATTTTATTTTCCCAGCAATTCAAGAAGAATCTCAAAGGTGTGAACGGAGGAAATGACTTTGATCAAGATATGCTGGAAGACATCTACAATGCCATCAAG[T/C]TAGTGCTCATTGTCTTGTTGTTCTCTTGCAGTTGTTGCTCTTTCTAATGCATAAAATGGGGGAGATGTTTATTACAATACATTTTTTCACTGATAAGTTTTTGTATAAAATAAAATTCTTTGTGAATAAAACCATGCTTATACAGACCCCCTAGTTTTTCACAATTTTTTTATTTTTCGCTAAAAAATGACTGATTTATTGGTGGTAATTCCCAGATATTTGCAGACAATTTTGCAATTACAAAAAAAATAAAATAAATAAAAATAACTGAATCTGATTGGCTGATAGCTGTGCGATATTTTGCCAGTAACAACACCGCCCACGTACAGCAAGCAACAAGCAGAGACCCTACAGTTTGACAAATATTACTGTTGTTAGATAACAAAATGTATTTTTGAGGCTTTTTTAGTGGAGAATGTAGTTGTTTAGATTGCAACTATGCAGTTTATTTGCAAGAATAGTGCCTATTTTAAAATATTTACAATTTCTGAGAGCTCGTC
Associated Phenotype:
Not determined